{{Rsnum
|rsid=121434589
|Chromosome=17
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=MYH2
|position=10535137
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MYH2
}}{{omim
|id=160740
|rsnum=121434589
|variant=0001
}}{{ClinVar
|rsid=121434589
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=10438454
|CHROM=17
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=MYH2:4620
|GENE_NAME=MYH2
|GENE_ID=4620
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.10438454C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=160740.0001
|CLNSIG=5
|CLNCUI=C1854106
|CLNDBN=Inclusion body myopathy 3
|Disease=Inclusion body myopathy 3
|CLNACC=RCV000015199.24
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1854106:605637:79091
}}